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急性口服卡托普利可抑制人脑脊液中的血管紧张素转换酶活性。

Acute oral captopril inhibits angiotensin converting enzyme activity in human cerebrospinal fluid.

作者信息

Geppetti P, Spillantini M G, Frilli S, Pietrini U, Fanciullacci M, Sicuteri F

出版信息

J Hypertens. 1987 Apr;5(2):151-4. doi: 10.1097/00004872-198704000-00004.

Abstract

Angiotensin converting enzyme (ACE) activity in human plasma and cerebrospinal fluid (CSF), was measured by a fluorimetric method, following an acute oral dose (75 mg) of captopril. A decrease of approximately 60% in enzyme activity was observed in CSF, suggesting that the drug penetrates the blood/brain barrier (BBB) in sufficient amounts to inhibit the ACE in CSF. The activity of CSF enkephalinase, an enzyme present in human brain and inhibited in vitro by an elevated concentration of captopril, was, however, unaffected by the acute drug administration. It is proposed that the antihypertensive effect of captopril in humans may be due, at least in part, to the inhibition of ACE contained within brain structures.

摘要

采用荧光法测定了急性口服剂量(75毫克)卡托普利后人体血浆和脑脊液(CSF)中的血管紧张素转换酶(ACE)活性。在脑脊液中观察到酶活性下降了约60%,这表明该药物能够以足够的量穿透血脑屏障(BBB),从而抑制脑脊液中的ACE。然而,脑脊液脑啡肽酶(一种存在于人类大脑中且在体外会被高浓度卡托普利抑制的酶)的活性并未受到急性给药的影响。有人提出,卡托普利对人类的降压作用可能至少部分归因于对脑结构中所含ACE的抑制。

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